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Table representation of search results timeline featuring number of search results per year.
Year | Number of Results |
---|---|
2003 | 1 |
2005 | 1 |
2006 | 1 |
2018 | 1 |
2019 | 1 |
2020 | 1 |
2021 | 1 |
2024 | 0 |
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Page 1
Genomic deletions in MSH2 or MLH1 are a frequent cause of hereditary non-polyposis colorectal cancer: identification of novel and recurrent deletions by MLPA.
Hum Mutat. 2003 Dec;22(6):428-33. doi: 10.1002/humu.10291.
Hum Mutat. 2003.
PMID: 14635101
Molecular characterization of the spectrum of genomic deletions in the mismatch repair genes MSH2, MLH1, MSH6, and PMS2 responsible for hereditary nonpolyposis colorectal cancer (HNPCC).
van der Klift H, Wijnen J, Wagner A, Verkuilen P, Tops C, Otway R, Kohonen-Corish M, Vasen H, Oliani C, Barana D, Moller P, Delozier-Blanchet C, Hutter P, Foulkes W, Lynch H, Burn J, Möslein G, Fodde R.
van der Klift H, et al.
Genes Chromosomes Cancer. 2005 Oct;44(2):123-38. doi: 10.1002/gcc.20219.
Genes Chromosomes Cancer. 2005.
PMID: 15942939
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A de novo MLH1 germ line mutation in a 31-year-old colorectal cancer patient.
Plasilova M, Zhang J, Okhowat R, Marra G, Mettler M, Mueller H, Heinimann K.
Plasilova M, et al.
Genes Chromosomes Cancer. 2006 Dec;45(12):1106-10. doi: 10.1002/gcc.20374.
Genes Chromosomes Cancer. 2006.
PMID: 16955466
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Molecular and presymptomatic analysis of a Moroccan Lynch syndrome family revealed a novel frameshift MLH1 germline mutation.
Moufid FZ, Bouguenouch L, El Bouchikhi I, Houssaini MI, Ouldim K.
Moufid FZ, et al.
Turk J Gastroenterol. 2018 Nov;29(6):701-704. doi: 10.5152/tjg.2018.17761.
Turk J Gastroenterol. 2018.
PMID: 30289396
Free PMC article.
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Whole-exome sequencing identified a novel mutation of MLH1 in an extended family with lynch syndrome.
Ghaedi H, Ramsheh SM, Omidvar ME, Labbaf A, Alehabib E, Akbari S, Pourfatemi F, Darvish H.
Ghaedi H, et al.
Genes Dis. 2019 Jul 27;7(4):614-619. doi: 10.1016/j.gendis.2019.07.011. eCollection 2020 Dec.
Genes Dis. 2019.
PMID: 33335961
Free PMC article.
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A rare large duplication of MLH1 identified in Lynch syndrome.
Kumar A, Paramasivam N, Bandapalli OR, Schlesner M, Chen T, Sijmons R, Dymerska D, Golebiewska K, Kuswik M, Lubinski J, Hemminki K, Försti A.
Kumar A, et al.
Hered Cancer Clin Pract. 2021 Jan 19;19(1):10. doi: 10.1186/s13053-021-00167-0.
Hered Cancer Clin Pract. 2021.
PMID: 33468175
Free PMC article.
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